Method Validation

Aptar Pharma's specialized analytical, development and regulatory services contribute value throughout the entire drug development process, expediting progress and mitigating risks along the journey.

From pre-clinical development to commercial supply, Patheon by Thermo Fisher Scientific is an industry leader in the development and manufacture of mammalian cell culture drug substances. Patheon offers biotech and pharmaceutical companies the ability to pursue opportunities around the globe with a fully i...

Avéma has a full analytical lab, staffed by experienced professionals with more than 200 years of method development and validation experience.

Quality management systems (QMS) are crucial for the success of any business. They provide an accurate way to track and measure quality across all areas of your company. One key benefit of a quality management system is that it establishes clear goals, roles, and responsibilities. It also tracks the pr...

Services for the development of inhalation drugs: Our team have over 30 years of experience supporting our clients' product development for orally inhaled or nasal drug products (OINDP). This includes formulation, stability, testing, product performance testing, in vitro bioequivalence studies, CMC...

To accelerate the development and marketing of your Biotherapeutics, Quality Assistance offers a complete analytical package to meet the EMA and FDA requirements, all on one site.

Whether it is to extend your analytical capacities or to outsource parts or all of your analytical needs, ...

Innovation & Formulation: We offer pharmaceutical R&D, feasibility studies, proof-of-concept, formulation development and analytical method development for multiple dosage forms such as solids, semi-solids, liquids, oral films, and transdermal patches. We can work with over 30 pharma technologies f...

Pharmaffiliates is providing all the Analytical Services (i.e. Method Development, Method Validation & Transfer, Stability Studies, Contract Analysis, etc)

QACS Lab is GMP certified and provides contract laboratory testing for Pharmaceuticals. Methodologies stay in accordance with EMA & FDA. QACS is equipped with Microbiological - Chemical - Molecular - Packaging laboratory premises to provide variety of Pharmaceutical testing solutions &am...

Nelson Labs offers a full trifecta of services to meet the requirements of ISO 10993 for Extractables & Leachables, Biocompatibility and Toxicological Assessments of medical devices. Biocompatibility testing is very common in the medical device industry. However, with 24 possible categories, each with a u...

De l'idée à la conception, l'industrialisation jusqu'à la qualification et la production.
From the idea trough the design, industrialization until qualification and production.

By the end of 2017 we will have a MHRA, GMP licenced laboratory. We will be offering a wide range of services for routine Quality Control analysis including QC release testing, method validation and stability analysis (analytical and microbiological). We work to the highest standards of GMP and GLP with r...

Curida offers Lab services1 chemical lab 
3 microbiological labs, including sterility lab and lab for test organisms


Main services:
Quality Control 
Method development and validation 
Stability testing 
Contract laboratory

testo Saveris - Data monitoring systems with automated and uninterrupted measurement data recording of temperature and humidity values in the environment and in processes. Offers centralized documentation as well as an alarm function thusly saving time. It guarantees the safety of your measurement data...

• Multiple MOC swab frame • Multiple MOC swab frame with handle • Telescopic device for holding swab frame • Telescopic device for holding swab stick • Telescopic device with mirror and torch • Multiple MOC swab templates

Pharmaceutical companies must be capable of delivering products to the market with the utmost level of quality and safety. At Zamann Pharma Support, we have been aiding large and mid‐sized pharmaceutical companies in solving quality and compliance challenges while ensuring that practicality and qualit...

Validation of computerized systems (CSV) according to GxP Guidelines has been a basic requirement in the life science industry for many years now. However, as the complexity of the IT landscape and the degree of automation has increased, the effort required to keep compliance has risen as well. Of cour...

The validation of a new GxP software is only one part of a vast deployment process. Preparation in the form of new processes, validation documentation, user management systems, life cycle management and training is always needed to ensure fresh software packages are fully compliant. At Zamann Ph...

Analytical methods development and validation: Our method development scientists work with a broad range of products, methods, and analytical technologies (chromatography, mass spectrometry, spectroscopy, biophysical analysis, bioanalytical techniques, etc.) to ensure that the method will meet its int...